Please use this identifier to cite or link to this item: http://dspace.utpl.edu.ec/handle/123456789/19000
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dc.contributor.authorGuaya Caraguay, D.es_ES
dc.contributor.authorFarran, A.es_ES
dc.contributor.authorValderrama, C.es_ES
dc.contributor.authorCortina, J.es_ES
dc.date.accessioned2017-06-16T22:02:46Z-
dc.date.available2017-06-16T22:02:46Z-
dc.date.issued2016-06-01es_ES
dc.date.submitted20/07/2015es_ES
dc.identifier10.1002/jctb.4763es_ES
dc.identifier.isbn2682575es_ES
dc.identifier.other10.1002/jctb.4763es_ES
dc.identifier.urihttp://dspace.utpl.edu.ec/handle/123456789/19000-
dc.description.abstractBACKGROUND: The incorporation of Fe(III) was performed in a natural clinoptilolite (Z-N) for simultaneous phosphate and ammonium removal. RESULTS: The existence of hydroxyl groups (?Fe-OH) in the iron zeolite (Z-Fe) enhances the phosphate uptake from 0.6�0.1mg-P g-1 in Z-N to 3.4�0.2mg-P g-1 in Z-Fe. However, the ammonium sorption capacity slightly decreases from 33�2mg-Ng-1 in Z-N to 27�2mg-Ng-1 in Z-Fe. The equilibrium and kinetics sorption were well explained by the Langmuir isotherm and the intraparticle diffusion model, respectively. CONCLUSIONS: Both the phosphate and ammonium uptake were slightly affected by the coexistence of competing ions. The phosphate sorption capacity of iron zeolite was decreased in the regeneration cycles. Desorption using a 1molL-1 NaOH solution under dynamic conditions provided higher enrichment factors for ammonium than phosphate. © 2015 Society of Chemical Industry.es_ES
dc.languageIngléses_ES
dc.subjectAmmoniumes_ES
dc.subjectClinoptilolitees_ES
dc.subjectIrones_ES
dc.subjectKinetices_ES
dc.subjectPhosphatees_ES
dc.subjectSorptiones_ES
dc.titleModification of a natural zeolite with Fe(III) for simultaneous phosphate and ammonium removal from aqueous solutionses_ES
dc.typeArticlees_ES
dc.publisherJournal of Chemical Technology and Biotechnologyes_ES
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